No abstract

Silicon nanocrystals (Si-ncs) are excellent candidates for the development of optoelectronic devices. Nevertheless, different strategies are still necessary to enhance their photo and electroluminescent properties by controlling their structural and compositional properties. In this work, the effect of the stoichiometry and structure on the optical properties of silicon rich oxide (SRO) films in a multilayered (ML) structure is studied. SRO MLs with silicon excess gradually increased towards the top and bottom and towards the center of the ML produced through the variation of the stoichiometry in each SRO layer were fabricated and confirmed by X-ray photoelectron spectroscopy. Si-ncs with three main sizes were observed by a transmission electron microscope, in agreement with the stoichiometric profile of each SRO layer. The presence of the three sized Si-ncs and some oxygen related defects enhances intense violet/blue and red photoluminescence (PL) bands. The SRO MLs were super-enriched with additional excess silicon by Si+ implantation, which enhanced the PL intensity. Oxygen-related defects and small Si-ncs (<2 nm) are mostly generated during ion implantation enhancing the violet/blue band to become comparable to the red band. The structural, compositional, and luminescent characteristics of the multilayers are the result of the contribution of the individual characteristics of each layer.

Heat transfer phenomena in multilayer structures have gained interest due to their promising use in thermal insulation and thermoelectricity applications. In such systems, nanostructuring has been used to introduce moderate interfacial density, and it has been demonstrated that interfacial thermal resistance plays a crucial role in reducing thermal conductivity κ. Nevertheless, the main constraint for actual applications is related to their tiny size because they are extremely thin to establish appreciable temperature gradients. In this work, by severe plastic deformation process of accumulative roll bonding (ARB), a 250 µm thick Cu‑Nb multilayer containing more than 8000 interfaces with periods below 40 nm was obtained, enabling the production of bulk metallic nanolaminates with ultralow κ. Multilayers present an ultralow κ of ~0.81 W/mK at 300 K, which is 100 times smaller than its Cu‑Nb bulk counterpart, and even lower than the amorphous lattice limit for the Cu‑Nb thin film system. By using electron diffusive mismatch model (EDMM), we argue that both electrons diffusively scattering at interface and those ballistically crossing the constituents are responsible for heat conduction in the Cu‑Nb multilayers at nanoscale. Hence, ARB Cu‑Nb multilayers are intriguing candidate materials which can prove avenues to achieve stable ultralow κ thermal barriers for robust applications.

The measurement of local temperature in nanoscale volumes is becoming a technological frontier. Photoluminescent nanoparticles and nanocolloids are the natural choice for nanoscale temperature probes. However, the influence of a surrounding liquid on the cryogenic behavior of oxidized Si-nanocrystals (Si-NCs) has never been investigated. In this work, the photoluminescence (PL) of oxidized Si-NCs/alcohol based nanocolloids is measured as a function of the temperature and the molecule length of monohydric alcohols above their melting-freezing point. The results unveil a progressive blue shift on the emission peak which is dependent on the temperature as well as the dielectric properties of the surrounding liquid. Such an effect is analyzed in terms of thermal changes of the Si-NCs bandgap, quantum confinement and the polarization effects of the embedding medium; revealing an important role of the dielectric constant of the surrounding liquid. These results are relevant because they offer a general insight to the fundamental behavior of photoluminescent nanocolloids under a cooling process and moreover, enabling PL tuning based on the dielectric properties of the surrounding liquid. Hence, the variables required to engineer PL of nanofluids are properly identified for use as temperature sensors at the nanoscale.

Partially functionalized carbon fibers with phase change organic molecules are newfangled candidate materials which can provide avenues to achieve high performance thermal rectifiers with a novel architecture via surface chemical functionalization.